Clinical Trial Protocol Specialist
India, Remote 求人ID R0000015412 Category Medical WritingAbout this Role
Clinical Trial Protocol Specialist
- The Clinical Trial Protocol Specialist will research, create, and edit clinical trial protocols as well as provide expert support for protocol development.
- Operates as a lead medical writer or as a Subject Matter Expert (SME) to support Medical Writers and Clinical Trial Services management, as well as other Parexel functions.
- Facilitates process improvement by participating in protocol development initiatives.
- The Clinical Trial Protocol Specialist may also support Medical Writing Services management during the sales process by providing client liaison and proposals input.
- The writers must have at least 5 years of overall writing experience, specifically Clinical trial protocol writing experience, with at least 5-10 protocols in the last year, and/or protocol design experience.
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